Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants

BACKGROUND: Retinitis Pigmentosa (RP) is a clinically and genetically heterogeneous disorder that results in inherited blindness. Despite the large number of genes identified, only ~ 60% of cases receive a genetic diagnosis using targeted-sequencing. The aim of this study was to design a whole genom...

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Detalles Bibliográficos
Autores principales: González-del Pozo, María, Fernández-Suárez, Elena, Martín-Sánchez, Marta, Bravo-Gil, Nereida, Méndez-Vidal, Cristina, Rodríguez-de la Rúa, Enrique, Borrego, Salud, Antiñolo, Guillermo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014749/
https://www.ncbi.nlm.nih.gov/pubmed/32050993
http://dx.doi.org/10.1186/s12967-020-02258-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014749/
https://www.ncbi.nlm.nih.gov/pubmed/32050993
http://dx.doi.org/10.1186/s12967-020-02258-3

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